上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。
MI-136 纯度: 98.64%
MI-136 是 menin-MLL (PPI) 蛋白互作的抑制剂,其 IC50 值为31 nM,Kd 值为23.6 nM。MI-136 可抑制 AR 信号通路,有用于去势抵抗性肿瘤的潜能。
MI-136 Chemical Structure
CAS No. : 1628316-74-4
规格 | 价格 | 是否有货 | 数量 |
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Free Sample (0.1-0.5 mg) | Apply now | ||
10 mM * 1 mL in DMSO | ¥1160 | In-stock | |
5 mg | ¥1050 | In-stock | |
10 mg | ¥1800 | In-stock | |
50 mg | ¥6500 | In-stock | |
100 mg | ¥11250 | In-stock | |
200 mg | 询价 | ||
500 mg | 询价 |
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MI-136 相关产品
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- Reprogramming Compound Library
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- Transcription Factor Targeted Library
生物活性 |
MI-136 is an inhibitor of the menin-MLL protein-protein interaction (PPI), with an IC50 of 31 nM and a Kd of 23.6 nM. MI-136 shows to block AR signaling and has the potential for the study in castration-resistant tumors[1][2]. |
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体外研究 (In Vitro) |
MI-136 (0-20) exhibits IC50values of 5.59 μM, 7.15 μM, 5.37 μM and 19.76 μM in LNCaP, VCaP, 22rv1 and PNT2 cells[2]. 上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only. Cell Proliferation Assay[2]
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体内研究 (In Vivo) |
MI-136 exhibits T1/2 of 3.1 h after po administration[1]. 上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only.
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分子量 |
470.51 |
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Formula |
C23H21F3N6S |
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CAS 号 |
1628316-74-4 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
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溶解性数据 |
In Vitro:
DMSO : 110 mg/mL (233.79 mM; Need ultrasonic) 配制储备液
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请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 In Vivo:
请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
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参考文献 |
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